| Literature DB >> 29233040 |
Ningxia Xie1,2, Polina Vikhreva1, Margherita Annicchiarico-Petruzzelli3, Ivano Amelio1, Nicolai Barlev4, Richard A Knight1, Gerry Melino1,2,4.
Abstract
As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.Entities:
Keywords: Integrins; adhesion and migration; cancer cells; cell interaction; oncogenes and tumor suppressors; oncosupression; p53 family; p73; transcription factors
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Year: 2018 PMID: 29233040 PMCID: PMC5969564 DOI: 10.1080/15384101.2017.1403684
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534